5'-Flanking region polymorphism of the neuronal nitric oxide synthase gene with Parkinson's disease in TaiwanLO, Hsiao-Sui; HOGAN, Edward L; SOONG, Bing-Wen et al.Journal of the neurological sciences. 2002, Vol 194, Num 1, pp 11-13, issn 0022-510XArticle

Dentatorubropallidoluysian atrophy in ChineseLEE, I-Hui; SOONG, Bing-Wen; LU, Yi-Chun et al.Archives of neurology (Chicago). 2001, Vol 58, Num 11, pp 1905-1908, issn 0003-9942Article

Frequency analysis of autosomal dominant cerebellar ataxias in Taiwanese patients and clinical and molecular characterization of Spinocerebellar ataxia type 6SOONG, Bing-Wen; LU, Yi-Chun; CHOO, Kong-Bung et al.Archives of neurology (Chicago). 2001, Vol 58, Num 7, pp 1105-1109, issn 0003-9942Article

Use of diffusion tensor imaging to identify similarities and differences between cerebellar and Parkinsonism forms of multiple system atrophyWANG, Po-Shan; WU, Hsiu-Mei; LIN, Ching-Po et al.Neuroradiology (Berlin. Print). 2011, Vol 53, Num 7, pp 471-481, issn 0028-3940, 11 p.Article

Regional patterns of cerebral glucose metabolism in spinocerebellar ataxia type 2, 3 and 6 : A voxel-based FDG-positron emission tomography analysisWANG, Po-Shan; LIU, Ren-Shyan; YANG, Bang-Hung et al.Journal of neurology. 2007, Vol 254, Num 7, pp 838-845, issn 0340-5354, 8 p.Article

A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome lp21-q23CHUNG, Ming-Yi; LU, Yi-Chun; CHENG, Nai-Chia et al.Brain. 2003, Vol 126, pp 1293-1299, issn 0006-8950, 7 p., 6Article

Spinocerebellar ataxia 35: Novel mutations in TGM6 with clinical and genetic characterizationGUO, Yuh-Cherng; LIN, Juei-Jueng; LIAO, Yi-Chu et al.Neurology. 2014, Vol 83, Num 17, pp 1554-1561, issn 0028-3878, 8 p.Article

Transmissible spongiform encephalopathies with P102L mutation of PRNP manifesting different phenotypes: clinical, neuroimaging, and electrophysiological studies in Chinese kindred in TaiwanCHI, Nai-Fang; LEE, Yi-Chung; LU, Yi-Chun et al.Journal of neurology. 2010, Vol 257, Num 2, pp 191-197, issn 0340-5354, 7 p.Article

Polymorphism distribution of prion protein codon 117, 129 and 171 in TaiwanWANG, Kaw-Chen; WANG, Vinchi; SUN, Ming-Chieh et al.European journal of epidemiology. 2007, Vol 22, Num 4, pp 257-261, issn 0393-2990, 5 p.Article

Metabolic characterization of Spinocerebellar ataxia type 6SOONG, Bing-Wen; LIU, Ren-Shyan; WU, Liang-Chih et al.Archives of neurology (Chicago). 2001, Vol 58, Num 2, pp 300-304, issn 0003-9942Article

Creutzfeldt-Jakob disease : heat shock protein 70 mRNA levels in mononuclear blood cells and clinical studySHYU, Woei-Cherng; KAO, Ming-Ching; CHOU, Wei-Yuan et al.Journal of neurology. 2000, Vol 247, Num 12, pp 929-934, issn 0340-5354Article

Comparison of Cerebellar Ataxias: A Three-Year Prospective Longitudinal AssessmentLEE, Yi-Chung; LIAO, Yi-Chu; WANG, Po-Shan et al.Movement disorders. 2011, Vol 26, Num 11, pp 2081-2087, issn 0885-3185, 7 p.Article

A novel ABCD1 gene mutation in a chinese-taiwanese patient with adrenomyeloneuropathyLIU, Yo-Tsen; LIN, Kang-Hsu; SOONG, Bing-Wen et al.Pediatric neurology. 2007, Vol 36, Num 5, pp 348-350, issn 0887-8994, 3 p.Article

Polymorphic Ala-allele carriers at residue 1170 of HER2 associated with Parkinson's diseaseVINCHI WANG; CHUANG, Tzu-Chao; KAO, Ming-Ching et al.Journal of the neurological sciences. 2013, Vol 325, Num 1-2, pp 115-119, issn 0022-510X, 5 p.Article

Median nerve motor conduction velocity is concordant with myelin protein zero gene mutationLEE, Yi-Chung; SOONG, Bing-Wen; LIU, Yo-Tsen et al.Journal of neurology. 2005, Vol 252, Num 2, pp 151-155, issn 0340-5354, 5 p.Article

Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonismSHAN, Din-E; SOONG, Bing-Wen; SUN, Chen-Ming et al.Annals of neurology. 2001, Vol 50, Num 6, pp 812-815, issn 0364-5134Article

Dysregulation of C/EBPα by mutant huntingtin causes the urea cycle deficiency in huntington's diseaseCHIANG, Ming-Chang; CHEN, Hui-Mei; WU, Jer-Yuarn et al.Human molecular genetics (Print). 2007, Vol 16, Num 5, pp 483-498, issn 0964-6906, 16 p.Article

Multimodal evoked potentials of Kennedy's diseaseLAI, Tsu-Hsien; SOONG, Bing-Wen; CHEN, Jen-Tse et al.Canadian journal of neurological sciences. 2007, Vol 34, Num 3, pp 328-332, issn 0317-1671, 5 p.Article

Increased Gene Dosage of Myelin Protein Zero Causes Charcot-Marie-Tooth DiseaseMAEDA, Meiko Hashimoto; MITSUI, Jun; OKAMOTO, Tomoko et al.Annals of neurology. 2012, Vol 71, Num 1, pp 84-92, issn 0364-5134, 9 p.Article

Mutations in KCND3 Cause Spinocerebellar Ataxia Type 22LEE, Yi-Chung; DURR, Alexandra; LI, Jun Z et al.Annals of neurology. 2012, Vol 72, Num 6, pp 859-869, issn 0364-5134, 11 p.Article

Asian origin for the worldwide-spread mutational event in machado-joseph diseaseMARTINS, Sandra; CALAFELL, Francesc; SOONG, Bing-Wen et al.Archives of neurology (Chicago). 2007, Vol 64, Num 10, pp 1502-1508, issn 0003-9942, 7 p.Article

Expanded trinucleotide repeats in the TBP/SCA17 gene mapped to chromosome 6q27 are associated with schizophreniaCHEN, Chiung-Mei; LANE, Hsien-Yuan; SOONG, Bing-Wen et al.Schizophrenia research. 2005, Vol 78, Num 2-3, pp 131-136, issn 0920-9964, 6 p.Article

Clinical and cellular characterization of two novel MPZ mutations, p.I135M and p.Q187PfsX63LIN, Kon-Ping; SOONG, Bing-Wen; CHANG, Ming-Hong et al.Clinical neurology and neurosurgery (Dutch-Flemish ed.). 2012, Vol 114, Num 2, pp 124-129, issn 0303-8467, 6 p.Article

Impairments in Cognitive Function and Brain Connectivity in Severe Asymptomatic Carotid StenosisCHENG, Hsien-Lin; LIN, Chun-Jen; SOONG, Bing-Wen et al.Stroke (1970). 2012, Vol 43, Num 10, pp 2567-2573, issn 0039-2499, 7 p.Article

Cellular characterization of MPZ mutations presenting with diverse clinical phenotypesLEE, Yi-Chung; LIN, Kon-Ping; CHANG, Ming-Hong et al.Journal of neurology. 2010, Vol 257, Num 10, pp 1661-1668, issn 0340-5354, 8 p.Article